tert-Butylcyclohexane | C10H20 | CID 18508 - PubChem
tert-Butylcyclohexane | C10H20 | CID 18508 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
Cyclohexane, (1,1-dimethylethyl)- - NIST Chemistry WebBook
In addition to the Thermodynamics Research Center (TRC) data available from this site, much more physical and chemical property data is available from the following TRC products: SRD 103a – Thermo Data Engine (TDE) for pure compounds. Go To: Top, Phase change data, Notes.
Structure of TERT-BUTYLCYCLOHEXANE (C10H20) - Mol-Instincts
TERT-BUTYLCYCLOHEXANE contains total 30 bond (s); 10 non-H bond (s), 1 rotatable bond (s), and 1 six-membered ring (s). Learn more about chemical structure at Mol-Instincts.
Cyclohexane, (1,1-dimethylethyl)- - NIST Chemistry WebBook
Other names: Cyclohexane, tert-butyl-; tert-Butylcyclohexane; 1-tert-Butylcyclohexane; t-Butylcyclohexane; Cyclohexane, t-butyl- Permanent link for this species. Use this link for bookmarking this species for future reference.
Tert-butylcyclohexane | chemical compound | Britannica
99 percent of tert-butylcyclohexane molecules adopt chair conformations in which the (CH 3) 3 C― group is equatorial. Read More
Tert-butylcyclohexane | C10H20 - ChemSpider
ChemSpider record containing structure, synonyms, properties, vendors and database links for Tert-butylcyclohexane, 3178-22-1
Desymmetrization of cyclohexanes by site- and stereoselective …
2018年12月19日 · We first examined tert -butylcyclohexane as our model substrate. With the bulky tert -butyl group in the preferred equatorial position, there exist 11 different C–H bonds—excluding primary...
tert-Butylcyclohexane ≥99% | Sigma-Aldrich - MilliporeSigma
tert-Butylcyclohexane ≥99%; CAS Number: 3178-22-1; EC Number: 221-652-4; Synonyms: 2-Cyclohexyl-2-methylpropane; Linear Formula: (C6H11)C(CH3)3 at Sigma-Aldrich
11.9: The E2 Reaction and Cyclohexane Conformation
Which isomer would be expected to undergo E2 elimination quicker cis or trans-1-bromo-4-tert-butylcyclohexane? Explain your answer.
4.8: Conformations of Disubstituted Cyclohexanes
Solving for the equilibrium constant K shows that the equatorial is preferred about 460:1 over axial. This means that 1-tert-butyl-1-methylcyclohexane will spend the majority of its time in the more stable conformation, with the tert-butyl group in the equatorial position.